Evidence map›Paper›PMID 8319975›Full record

ArticleImmunogenetics1993

Organization and structure of the H-2M4-M8 class I genes in the mouse major histocompatibility complex.

C R Wang, K F Lindahl

Abstract read
PubMed Publisher
In one paragraph

Article in Immunogenetics, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. BAC clones and STS markers near the distal breakpoint of the fourth t-inversion, In(17)4d, in the H2-M region on mouse chromosome 17.Mammalian genome : official journal of the International Mammalian Genome Society · 1998
    Article
  7. Article
  8. Article
  9. Mapping of 12 markers in the proximal region of mouse chromosome 17 using recombinant t haplotypes.Mammalian genome : official journal of the International Mammalian Genome Society · 1995
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. A second lineage of mammalian major histocompatibility complex class I genes.Proceedings of the National Academy of Sciences of the United States of America · 1994
    Article
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

C R WangHoward Hughes Medical Institute, Department of Microbiology, University of Texas Southwestern Medical Center, Dallas 75235-9050.
K F Lindahl

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have cloned and characterized five new class I genes from the M region at the distal end of the H-2 complex of the BALB/c mouse. M4, M5, and M6 are clustered on two overlapping cosmids, and M7 and M8 are located on another cosmid together with the previously cloned M1 gene, to which they are most closely related. M4, M6, and M7 are full-length class I genes (exons 1 through 5 were identified) but with stop codons or frameshifts that mark them as pseudogenes, and only exons 4 and 5 remain of M8. M5 has complete open reading frames in exons 1 through 5 and intact splice signals; it has the potential to encode a divergent class I major histocompatibility molecule, but no transcripts were found. These genes provide probes for studying the evolution of class I genes in rodents and for the mapping and cloning of genes at the end of the distal inversion in t haplotype chromosomes.

Indexed as

Genes, MHC Class IAmino Acid SequenceAnimalsBase SequenceChromosome MappingCloning, MolecularDNAH-2 AntigensMiceMice, Inbred BALB CMice, Inbred C3HMolecular Sequence DataDNAH-2 Antigens

Identifiers

PMID8319975

What OpenQuestion holds

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Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.